Product Recalls in Arkansas
Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,535 recalls have been distributed to Arkansas in the last 12 months.
Showing 17301–17320 of 28,355 recalls
Recalled Item: ArrowADVANTAGE 5 Pressure Injectable Peripherally Inserted Central Catheter...
The Issue: Finished good kits may contain incorrect components. Kits that should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium VR DF4 1240 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew POLARSTEM(TM) Femoral Stems with Ti/HA (Standard Recalled by...
The Issue: The Cardan joint of the Polarstem Cardan could potentially fracture or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUOHY Epidural Needle Recalled by Epimed International Due to Potential for...
The Issue: Potential for partially incomplete seal of product, impacting sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium DR 1510 Recalled by Sorin Group Italia SRL - CRF Due to There is a...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium VR 1210 Recalled by Sorin Group Italia SRL - CRF Due to There is a...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium DR DF4 1540 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COUDE Blunt Nerve Block Needle Recalled by Epimed International Due to...
The Issue: Potential for partially incomplete seal of product, impacting sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium CRT-D 1741 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX-2 COUDE Epidural Needle Recalled by Epimed International Due to Potential...
The Issue: Potential for partially incomplete seal of product, impacting sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium CRT DF1 1711 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAamp DSP Virus Kit Cat. No. 60704 Recalled by Qiagen, GmbH Due to Certain...
The Issue: Certain lots of the QIAamp DSP Virus Kit, , used in analytic workflows could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Direct Swish Duo-Grip Healing Collar Recalled by Implant Direct...
The Issue: The Swish Duo-Grip Healing Collar part number 9048-13H (4.8mm) package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FUJINON ED-530XT. This device is intended for the visualization of Recalled...
The Issue: An update to the design and labeling was implemented to help reduce patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accolade and Restoration hip product Recalled by Howmedica Osteonics Corp....
The Issue: Inner and outer sterile barriers not fully sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accolade and Restoration hip product Recalled by Howmedica Osteonics Corp....
The Issue: Inner and outer sterile barriers not fully sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sekisui Diagnostics Sekure Chemistry Acetaminophen L3K Recalled by Beckman...
The Issue: Reagent carryover from Sekisui ACTH when utilized on the BEC AU 680 analyzer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Elastic Esmark Bandage Recalled by Medline Industries Inc Due to...
The Issue: Product did not undergo correct sterilization procedures and may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife(TM) Reduced Heparin ARTERIAL BLOOD SAMPLER Recalled by Vyaire...
The Issue: Lot #0001047501 of the 9025RHTR ABG sampling kits have been manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas 6000 Modular Series system Recalled by Roche Diagnostics Corporation...
The Issue: A warning is being added to the cobas¿ 6000 MODULAR Series System - c501 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.